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4. A new genetic locus for X linked progressive cone-rod dystrophy. Jalkanen R; Demirci FY; Tyynismaa H; Bech-Hansen T; Meindl A; Peippo M; Mäntyjärvi M; Gorin MB; Alitalo T J Med Genet; 2003 Jun; 40(6):418-23. PubMed ID: 12807962 [TBL] [Abstract][Full Text] [Related]
6. A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13. Balciuniene J; Johansson K; Sandgren O; Wachtmeister L; Holmgren G; Forsman K Genomics; 1995 Nov; 30(2):281-6. PubMed ID: 8586428 [TBL] [Abstract][Full Text] [Related]
7. X-linked high myopia associated with cone dysfunction. Young TL; Deeb SS; Ronan SM; Dewan AT; Alvear AB; Scavello GS; Paluru PC; Brott MS; Hayashi T; Holleschau AM; Benegas N; Schwartz M; Atwood LD; Oetting WS; Rosenberg T; Motulsky AG; King RA Arch Ophthalmol; 2004 Jun; 122(6):897-908. PubMed ID: 15197065 [TBL] [Abstract][Full Text] [Related]
8. Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1). Hong HK; Ferrell RE; Gorin MB Am J Hum Genet; 1994 Dec; 55(6):1173-81. PubMed ID: 7977377 [TBL] [Abstract][Full Text] [Related]
9. X-linked cone dystrophy caused by mutation of the red and green cone opsins. Gardner JC; Webb TR; Kanuga N; Robson AG; Holder GE; Stockman A; Ripamonti C; Ebenezer ND; Ogun O; Devery S; Wright GA; Maher ER; Cheetham ME; Moore AT; Michaelides M; Hardcastle AJ Am J Hum Genet; 2010 Jul; 87(1):26-39. PubMed ID: 20579627 [TBL] [Abstract][Full Text] [Related]
10. Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy. Mäntyjärvi M; Nurmenniemi P; Partanen J; Myöhänen T; Peippo M; Alitalo T Acta Ophthalmol Scand; 2001 Aug; 79(4):359-65. PubMed ID: 11453854 [TBL] [Abstract][Full Text] [Related]
11. A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome. Assink JJ; Tijmes NT; ten Brink JB; Oostra RJ; Riemslag FC; de Jong PT; Bergen AA Am J Hum Genet; 1997 Oct; 61(4):934-9. PubMed ID: 9382106 [TBL] [Abstract][Full Text] [Related]
12. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation. Lines MA; Hébert M; McTaggart KE; Flynn SJ; Tennant MT; MacDonald IM Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607 [TBL] [Abstract][Full Text] [Related]
13. A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27. Gieser L; Fujita R; Göring HH; Ott J; Hoffman DR; Cideciyan AV; Birch DG; Jacobson SG; Swaroop A Am J Hum Genet; 1998 Nov; 63(5):1439-47. PubMed ID: 9792872 [TBL] [Abstract][Full Text] [Related]
14. Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3. Mulligan LM; Phillips MA; Forster-Gibson CJ; Beckett J; Partington MW; Simpson NE; Holden JJ; White BN Am J Hum Genet; 1985 May; 37(3):463-72. PubMed ID: 2988332 [TBL] [Abstract][Full Text] [Related]
15. Linkage mapping of a large Colombian family segregating for X linked retinoschisis: refinement of the chromosomal location. Shastry BS; Hejtmancik JF; Rodriguez A; Rodriguez F; Tamayo ML J Med Genet; 1997 Jun; 34(6):504-6. PubMed ID: 9192273 [TBL] [Abstract][Full Text] [Related]
16. Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3. Seymour AB; Dash-Modi A; O'Connell JR; Shaffer-Gordon M; Mah TS; Stefko ST; Nagaraja R; Brown J; Kimura AE; Ferrell RE; Gorin MB Am J Hum Genet; 1998 Jan; 62(1):122-9. PubMed ID: 9443860 [TBL] [Abstract][Full Text] [Related]
17. Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28. Yates JR; Warner JP; Smith JA; Deymeer F; Azulay JP; Hausmanowa-Petrusewicz I; Zaremba J; Borkowska J; Affara NA; Ferguson-Smith MA J Med Genet; 1993 Feb; 30(2):108-11. PubMed ID: 8445613 [TBL] [Abstract][Full Text] [Related]
18. Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter. Dlouhy SR; Christian JC; Haines JL; Conneally PM; Hodes ME Hum Genet; 1987 Feb; 75(2):136-9. PubMed ID: 3469136 [TBL] [Abstract][Full Text] [Related]
19. X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysis. Meire FM; Bergen AA; De Rouck A; Leys M; Delleman JW Br J Ophthalmol; 1994 Feb; 78(2):103-8. PubMed ID: 8123616 [TBL] [Abstract][Full Text] [Related]
20. Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree. Brown J; Kimura AE; Gorin MB Ophthalmology; 2000 Jun; 107(6):1104-10. PubMed ID: 10857830 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]